dc.contributor.author
Strassburger, David
dc.contributor.author
Herziger, Svenja
dc.contributor.author
Huth, Katharina
dc.contributor.author
Urschbach, Moritz
dc.contributor.author
Haag, Rainer
dc.contributor.author
Besenius, Pol
dc.date.accessioned
2021-03-12T14:34:03Z
dc.date.available
2021-03-12T14:34:03Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/29918
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-29660
dc.description.abstract
The synthesis of a sulfate-modified dendritic peptide amphiphile and its self-assembly into one-dimensional rod-like architectures in aqueous medium is reported. The influence of the ionic strength on the supramolecular polymerization was probed via circular dichroism spectroscopy and cryogenic transmission electron microscopy. Physiological salt concentrations efficiently screen the charges of the dendritic building block equipped with eight sulfate groups and trigger the formation of rigid supramolecular polymers. Since multivalent sulfated supramolecular structures mimic naturally occurring L-selectin ligands, the corresponding affinity was evaluated using a competitive SPR binding assay and benchmarked to an ethylene glycol-decorated supramolecular polymer.
en
dc.format.extent
8 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
L-selectin binders
en
dc.subject
multivalency
en
dc.subject
self-assembly in water
en
dc.subject
supramolecular polymers
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie::547 Organische Chemie
dc.title
Supramolecular polymerization of sulfated dendritic peptide amphiphiles into multivalent L-selectin binders
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.3762/bjoc.17.10
dcterms.bibliographicCitation.journaltitle
Beilstein Journal of Organic Chemistry
dcterms.bibliographicCitation.pagestart
97
dcterms.bibliographicCitation.pageend
104
dcterms.bibliographicCitation.volume
17
dcterms.bibliographicCitation.url
https://doi.org/10.3762/bjoc.17.10
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1860-5397
refubium.resourceType.provider
WoS-Alert